Chapman J - Search Results

1

Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200(Lys) mutation.

Chapman J, Arlazoroff A, Goldfarb LG, Cervenakova L, Neufeld MY, Werber E, Herbert M, Brown P, Gajdusek DC, Korczyn AD. Chapman J, et al. Neurology. 1996 Mar;46(3):758-61. doi: 10.1212/wnl.46.3.758. Neurology. 1996. PMID: 8618678

2

Transmission of spongiform encephalopathy from a familial Creutzfeldt-Jakob disease patient of Jewish Libyan origin carrying the PRNP codon 200 mutation.

Chapman J, Brown P, Rabey JM, Goldfarb LG, Inzelberg R, Gibbs CJ Jr, Gajdusek DC, Korczyn AD. Chapman J, et al. Neurology. 1992 Jun;42(6):1249-50. doi: 10.1212/wnl.42.6.1249-a. Neurology. 1992. PMID: 1351274 No abstract available.

3

Absence of prion protein mutation in bipolar manic-depressive patients.

Korczyn AD, Chapman J, Belmaker RH, Shimon H, Baron M. Korczyn AD, et al. Among authors: chapman j. Br J Psychiatry. 1992 Jul;161:132. doi: 10.1192/bjp.161.1.132. Br J Psychiatry. 1992. PMID: 1353393 No abstract available.

4

Antibodies from Down's syndrome patients bind to the same cholinergic neurofilament protein recognized by Alzheimer's disease antibodies.

Hassin-Baer S, Wertman E, Raphael M, Stark V, Chapman J, Michaelson DM. Hassin-Baer S, et al. Among authors: chapman j. Neurology. 1992 Mar;42(3 Pt 1):551-5. doi: 10.1212/wnl.42.3.551. Neurology. 1992. PMID: 1532232

5

Creutzfeldt-Jacob disease associated with the PRNP codon 200Lys mutation: an analysis of 45 families.

Goldfarb LG, Brown P, Mitrovà E, Cervenáková L, Goldin L, Korczyn AD, Chapman J, Gálvez S, Cartier L, Rubenstein R, et al. Goldfarb LG, et al. Among authors: chapman j. Eur J Epidemiol. 1991 Sep;7(5):477-86. doi: 10.1007/BF00143125. Eur J Epidemiol. 1991. PMID: 1684755

6

A mutation in the prion protein gene in Creutzfeldt-Jakob disease in Jewish patients of Libyan, Greek, and Tunisian origin.

Korczyn AD, Chapman J, Goldfarb LG, Brown P, Gajdusek DC. Korczyn AD, et al. Among authors: chapman j. Ann N Y Acad Sci. 1991;640:171-6. doi: 10.1111/j.1749-6632.1991.tb00211.x. Ann N Y Acad Sci. 1991. PMID: 1685643

7

Genetic and environmental factors determining the development of Creutzfeldt-Jakob disease in Libyan Jews.

Chapman J, Korczyn AD. Chapman J, et al. Neuroepidemiology. 1991;10(5-6):228-31. doi: 10.1159/000110276. Neuroepidemiology. 1991. PMID: 1798423

8

Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non-Libyan origin.

Goldfarb LG, Korczyn AD, Brown P, Chapman J, Gajdusek DC. Goldfarb LG, et al. Among authors: chapman j. Lancet. 1990 Sep 8;336(8715):637-8. doi: 10.1016/0140-6736(90)93443-s. Lancet. 1990. PMID: 1975415 No abstract available.

9

Routine and quantitative EEG analysis in Gilles de la Tourette's syndrome.

Neufeld MY, Berger Y, Chapman J, Korczyn AD. Neufeld MY, et al. Among authors: chapman j. Neurology. 1990 Dec;40(12):1837-9. doi: 10.1212/wnl.40.12.1837. Neurology. 1990. PMID: 2247231

10

Rats immunized with cholinergic synaptosomes: a model for Lambert-Eaton syndrome.

Chapman J, Rabinowitz R, Korczyn AD, Michaelson DM. Chapman J, et al. Muscle Nerve. 1990 Aug;13(8):726-33. doi: 10.1002/mus.880130811. Muscle Nerve. 1990. PMID: 2385259

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